4CPL
Structure of the Neuraminidase from the B/Brisbane/60/2008 virus.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04 |
Synchrotron site | Diamond |
Beamline | I04 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 159.784, 159.784, 91.592 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 46.126 - 2.000 |
R-factor | 0.1387 |
Rwork | 0.138 |
R-free | 0.16090 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1a4g |
RMSD bond length | 0.007 |
RMSD bond angle | 1.138 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.130 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.100 | 0.580 |
Number of reflections | 90807 | |
<I/σ(I)> | 15.84 | 4.2 |
Completeness [%] | 100.0 | 100 |
Redundancy | 7 | 7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 25% PEG 1500, 0.1M SUCCINIC ACID PH 9.0. |